Yao Jinjian, Yu Weiling, Chang Ying, Ren Jinghua, Xu Dong, Han Siyuan, Lin Jusheng
Institute of Liver Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
J Huazhong Univ Sci Technolog Med Sci. 2008 Jun;28(3):266-71. doi: 10.1007/s11596-008-0308-1. Epub 2008 Jun 19.
In order to screen potential mRNA locations of P gene in which targeting siRNAs can effectively inhibit HBV expression, 5 recombinant plasmids containing 4 targeting-specific siRNA fragments and a control were prepared and transfected into 2.2.15 cells respectively. The expression levels of HBx mRNA, HBs mRNA and HBc mRNA were detected by RT-PCR. The concentrations of the hepatitis B virus antigens, including HBsAg and HBeAg harvested from the culture supernatant of transfected 2.2.15 cells, were measured by ELISA. X protein was tested by Western blot. The results showed that four siRNAs against distinct mRNA locations of HBV polymerase gene had different inhibitory effects on their targeted mRNA. The plasmid-derived psiRNA1 and psiRNA2 could effectively inhibit the transcription and translation of HBs gene, whereas the inhibitory efficiency of psiRNA3, psiRNA4 for HBe gene was much higher than that of psiRNA1 and psiRNA2. In comparison to the rest of psiRNAs in this study, psiRNA4 was the most effective to suppress the transcription and translation of HBx. It is suggested that siRNA can be considered as a powerful therapeutic agent for reducing HBV expression. The siRNAs against HBV polymerase are effective largely depending on the location of targeted sites. To enhance inhibitory efficiency, hunting for high effective target in polymerase gene is necessary and feasible.
为筛选靶向小干扰RNA(siRNA)可有效抑制乙肝病毒(HBV)表达的P基因潜在信使核糖核酸(mRNA)位点,制备了5种重组质粒,分别包含4个靶向特异性siRNA片段和1个对照,并将其分别转染至2.2.15细胞中。采用逆转录聚合酶链反应(RT-PCR)检测X蛋白信使核糖核酸(HBx mRNA)、表面抗原信使核糖核酸(HBs mRNA)和核心抗原信使核糖核酸(HBc mRNA)的表达水平。采用酶联免疫吸附测定(ELISA)法检测从转染后的2.2.15细胞培养上清液中收获的乙肝病毒抗原,包括乙肝表面抗原(HBsAg)和乙肝e抗原(HBeAg)的浓度。通过蛋白质免疫印迹法检测X蛋白。结果显示,针对乙肝病毒聚合酶基因不同mRNA位点的4种siRNA对其靶向mRNA具有不同的抑制作用。质粒来源的小干扰RNA1(psiRNA1)和小干扰RNA2(psiRNA2)可有效抑制表面抗原基因(HBs)的转录和翻译,而小干扰RNA3(psiRNA3)、小干扰RNA4(psiRNA4)对e抗原基因(HBe)的抑制效率远高于psiRNA1和psiRNA2。与本研究中的其他psiRNA相比,psiRNA4在抑制X蛋白信使核糖核酸(HBx)的转录和翻译方面最为有效。提示siRNA可被视为一种强大的降低HBV表达的治疗剂。针对乙肝病毒聚合酶的siRNA的有效性很大程度上取决于靶位点的位置。为提高抑制效率,在聚合酶基因中寻找高效靶点是必要且可行的。